Divalproex Sodium 70518-3477-03

Package NDC

70518-3477-03

Manufacturer: Remedyrepack Inc.
Dosage Form: Tablet, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 16, 2022
Listing Expires: December 31, 2027
Application: ANDA209286

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Active Ingredients

Ingredient	Strength
Divalproex Sodium	500 mg/1

Drug Class

Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]

Selected Package

70518-3477-03Selected

100 POUCH in 1 BOX (70518-3477-3) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3477-4)

Other packages for this product(3)

70518-3477-00

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3477-0)

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70518-3477-01

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3477-1)

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70518-3477-05

100 POUCH in 1 BOX (70518-3477-5) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3477-6)

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